Variant #0000810430 (NC_000023.10:g.47434613C>T, NM_006950.3:c.1219G>A (SYN1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47434613C>T
DNA change (hg38) -
Published as SYN1(NM_006950.3):c.1219G>A (p.V407I)
ISCN -
DB-ID SYN1_000088
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 ?/. - c.*3757C>T r.(=) p.(=)
TIMP1 NM_003254.2 ?/. - c.-7269C>T r.(?) p.(=)
SYN1 NM_006950.3 ?/. - c.1219G>A r.(?) p.(Val407Ile)


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